Aripiprazole
- Product NDC
- 82804-023
- 11-digit product format
- 828040023
- Labeler code
- 82804
- Product ID
- 82804-023_fbd81df7-8482-493e-bfc5-a3352f466b9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aripiprazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203908
- Marketing category
- ANDA
- Marketing start
- 2015-10-08
- Substance
- ARIPIPRAZOLE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 82VFR53I78 | ARIPIPRAZOLE | 129722-12-9 | ARIPIPRAZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-023-30 | 82804002330 | 30 TABLET in 1 BOTTLE (82804-023-30) | 30 tablet | 2023-10-11 | No | No | Historical |
| 82804-023-60 | 82804002360 | 60 TABLET in 1 BOTTLE (82804-023-60) | 60 tablet | 2023-10-11 | No | No | Historical |
| 82804-023-90 | 82804002390 | 90 TABLET in 1 BOTTLE (82804-023-90) | 90 tablet | 2023-10-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Aripiprazole | Proficient Rx LP | 2023-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |